“…[9] These advantages have also been put to use in the field of solid-state ionics, viz., for production of composites with well-controlled mesostructure. [10][11][12] In our context, the benefits of using mesoporous materials is obvious: by loading the electrolyte matrix into a network of interconnected mesopores, as schematically shown in Figure 1b, the surface area of interfaces can be extended to values as high as 300-1000 m 2 g -1 , compared with 10-150 m 2 g -1 for fine insulator particles, [13] and a much higher volume fraction (compared to solid nanometer-sized particles) can be realized without losing percolation; both of these points lead to much higher ionic conductivities. As the size of ionic-conductor material loaded inside the pores is comparable to the Debye length (a few nanometers), consideration of mesoscopic effects on ionic conductivity due to overlapping space-charge regions becomes increasingly important.…”